Canonical Allele Identifier: CA2336431136

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41363702_41363703delinsGA , CM000681.2:g.41363702_41363703delinsGA GRCh38
NC_000019.9:g.41869607_41869608delinsGA , CM000681.1:g.41869607_41869608delinsGA GRCh37
NC_000019.8:g.46561447_46561448delinsGA NCBI36
NG_013091.1:g.5471_5472delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000243578.8:c.-4-180_-4-179delinsTC (B9D2) MANE Select ENSP00000243578.2:n.-4-180_-4-179delinsTC
ENST00000675972.1:c.-5+61_-5+62delinsTC (B9D2) ENSP00000501911.1:n.-5+61_-5+62delinsTC
ENST00000243578.7:c.-4-180_-4-179delinsTC (B9D2) ENSP00000243578.2:n.-4-180_-4-179delinsTC
ENST00000539627.5:c.-30+12500_-30+12501delinsGA (TMEM91) ENSP00000441900.1:n.-30+12500_-30+12501delinsGA
ENST00000594416.1:c.-4-180_-4-179delinsTC (B9D2) ENSP00000469666.1:n.-4-180_-4-179delinsTC
ENST00000601597.1:n.136-180_136-179delinsTC (B9D2)
ENST00000604123.5:c.142+9387_142+9388delinsGA (TMEM91) ENSP00000474871.1:n.142+9387_142+9388delinsGA
ENST00000604424.1:n.350+12500_350+12501delinsGA
NM_030578.3:c.-4-180_-4-179delinsTC (B9D2) NP_085055.2:n.-4-180_-4-179delinsTC
XM_006723405.1:c.-4-180_-4-179delinsTC (B9D2) XP_006723468.1:n.-4-180_-4-179delinsTC
XM_011527349.1:c.-5+61_-5+62delinsTC (B9D2) XP_011525651.1:n.-5+61_-5+62delinsTC
XM_011527350.1:c.-72+255_-72+256delinsTC (B9D2) XP_011525652.1:n.-72+255_-72+256delinsTC
XM_011527349.2:c.-5+61_-5+62delinsTC (B9D2) XP_011525651.1:n.-5+61_-5+62delinsTC
XM_011527350.2:c.-72+255_-72+256delinsTC (B9D2) XP_011525652.1:n.-72+255_-72+256delinsTC
NM_030578.4:c.-4-180_-4-179delinsTC (B9D2) MANE Select NP_085055.2:n.-4-180_-4-179delinsTC